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rs879255271

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs879255271(A;A)
Make rs879255271(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position1612357
GeneTCF3
is asnp
is mentioned by
dbSNPrs879255271
ebirs879255271
HLIrs879255271
Exacrs879255271
Varsomers879255271
Maprs879255271
PheGenIrs879255271
hapmaprs879255271
1000 genomesrs879255271
hgdprs879255271
ensemblrs879255271
gopubmedrs879255271
geneviewrs879255271
scholarrs879255271
googlers879255271
pharmgkbrs879255271
gwascentralrs879255271
openSNPrs879255271
23andMers879255271
23andMe allrs879255271
SNP Nexus

SNPshotrs879255271
SNPdbers879255271
MSV3drs879255271
GWAS Ctlgrs879255271
Max Magnitude0
ClinVar
Risk rs879255271(A;A)
Alt rs879255271(A;A)
Reference rs879255271(G;G)
Significance Pathogenic
Disease Agammaglobulinemia 8
Variation info
Gene TCF3
CLNDBN Agammaglobulinemia 8, autosomal dominant
Reversed 1
HGVS NC_000019.9:g.1612356C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000211091.1,